Canonical Allele Identifier: CA2690187578
Gene: FXN HGNC NCBI

Linked Data

gnomAD v4: 9-69035712-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69035712G>T , CM000671.2:g.69035712G>T GRCh38
NC_000009.11:g.71650628G>T , CM000671.1:g.71650628G>T GRCh37
NC_000009.10:g.70840448G>T NCBI36
NG_008845.2:g.5150G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377270.7:c.-71G>T ENSP00000366482.3:n.-71G>T
ENST00000396364.7:c.-71G>T ENSP00000379650.3:n.-71G>T
NM_000144.4:c.-71G>T NP_000135.2:n.-71G>T
NM_001161706.1:c.-71G>T NP_001155178.1:n.-71G>T
NM_181425.2:c.-71G>T NP_852090.1:n.-71G>T